• Cerebellar ependymoma with overlapping features of clear-cell and tanycytic variants mimicking hemangioblastoma: a case report and literature review
• Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p
• Contrast-enhancement in supratentorial low-grade gliomas: a classic prognostic factor in the molecular age
• Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis
• Discordant phenotypes in a mother and daughter with mosaic supernumerary ring chromosome 19 explained by a de novo 7q36.2 deletion and 7p22.1 duplication
• DNA structure modulates the oligomerization properties of the AAV initiator protein Rep68
• High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q
• Humoral deficiency in three paediatric patients with genetic diseases
• Impact of gross total resection in patients with WHO grade III glioma harboring the IDH 1/2 mutation without the 1p/19q co-deletion
• Loss of heterozygosity analysis in an anaplastic oligodendroglioma arising after radiation therapy
• Methylation of O6-methylguanine DNA methyltransferase and loss of heterozygosity on 19q and/or 17p are overlapping features of secondary glioblastomas with prolonged survival
• Prenatal diagnosis of minute supernumerary marker chromosomes
• Prognosis of oligodendroglial tumor with ring enhancement showing central necrotic portion
• Pure trisomy 19p syndrome in an infant with an extra ring chromosome
• Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring